Clinical relevance of FLT3 gene abnormalities in Brazilian patients with infant leukemia. - Wikidata - awgldk - TriplyDB

Clinical relevance of FLT3 gene abnormalities in Brazilian patients with infant leukemia.

Clinical relevance of FLT3 gene abnormalities in Brazilian patients with infant leukemia.

http://www.wikidata.org/entity/Q54783689

about

Revisiting the biology of infant t(4;11)/MLL-AF4+ B-cell acute lymphoblastic leukemia RAS mutations in early age leukaemia modulated by NQO1 rs1800566 (C609T) are associated with second-hand smoking exposures.Internal tandem duplication of the FLT3 gene confers poor overall survival in patients with acute promyelocytic leukemia treated with all-trans retinoic acid and anthracycline-based chemotherapy: an International Consortium on Acute Promyelocytic Le Demographic and prognostic factors of 455 patients with acute leukemia admitted to two referral hospitals in tehran-iran during ten years (2001-2011).FLT3 inhibitors in the treatment of acute myeloid leukemia: the start of an era?Investigational drugs targeting FLT3 for leukemia.The evolution of clinical trials for infant acute lymphoblastic leukemia.Molecular and cytogenetic abnormalities in acute myeloid leukemia: review and case studies.Prognostic significance of FLT3 mutational status and expression levels in MLL-AF4+ and MLL-germline acute lymphoblastic leukemia.Analysis of FLT3-ITD and FLT3-Asp835 mutations in de novo acute myeloid leukemia: evaluation of incidence, distribution pattern, correlation with cytogenetics and characterization of internal tandem duplication from Indian population.Clinical and molecular epidemiology of neonatal leukemia in Brazil.Ligand-independent FLT3 activation does not cooperate with MLL-AF4 to immortalize/transform cord blood CD34+ cells.Disease Characteristics and Prognostic Implications of Cell-Surface FLT3 Receptor (CD135) Expression in Pediatric Acute Myeloid Leukemia: A Report from the Children's Oncology Group.Impact of mutations in FLT3, PTPN11 and RAS genes on the overall survival of pediatric B cell precursor acute lymphoblastic leukemia in Brazil.

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Clinical relevance of FLT3 gene abnormalities in Brazilian patients with infant leukemia.

http://www.wikidata.org/entity/Q54783689

description

2008 nî lūn-bûn

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2008年の論文

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年學術文章

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2008年學術文章

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2008年學術文章

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name

Clinical relevance of FLT3 gene abnormalities in Brazilian patients with infant leukemia.

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Clinical relevance of FLT3 gene abnormalities in Brazilian patients with infant leukemia.

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type

label

Clinical relevance of FLT3 gene abnormalities in Brazilian patients with infant leukemia.

@en

Clinical relevance of FLT3 gene abnormalities in Brazilian patients with infant leukemia.

@nl

prefLabel

Clinical relevance of FLT3 gene abnormalities in Brazilian patients with infant leukemia.

@en

Clinical relevance of FLT3 gene abnormalities in Brazilian patients with infant leukemia.

@nl

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Leukemia & Lymphoma

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Clinical relevance of FLT3 gene abnormalities in Brazilian patients with infant leukemia

@en

P2093

Brazilian Collaborative Study Group of Infant Acute Leukemia

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Ilana Zalcberg

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Luiz Claudio Santos Thuler

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Marina Lipkin Vasquez

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P2860

Activating mutation of D835 within the activation loop of FLT3 in human hematologic malignancies.

A simple salting out procedure for extracting DNA from human nucleated cells

Establishment of a pediatric oncology program and outcomes of childhood acute lymphoblastic leukemia in a resource-poor area.

Analysis of FLT3-activating mutations in 979 patients with acute myelogenous leukemia: association with FAB subtypes and identification of subgroups with poor prognosis.

Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease.

Clinical heterogeneity in childhood acute lymphoblastic leukemia with 11q23 rearrangements.

Tyrosine kinase oncogenes in normal hematopoiesis and hematological disease.

The roles of FLT3 in hematopoiesis and leukemia.

Clinical implications of FLT3 mutations in pediatric AML.

MLL translocations specify a distinct gene expression profile that distinguishes a unique leukemia.

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2291-2297

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12

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49

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Maria S Pombo-de-Oliveira

Mariana Emerenciano

Juliane Menezes

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23567920

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